Clinical evaluation of idiopathic paroxysmal kinesigenic dyskinesia: New diagnostic criteria von BRUNO, M. K, HALLETT, M, SOONG, B.-W, ASHIZAWA, T, JANKOVIC, J, RENNER, D, FU, Y.-H, PTACEK, L. J, GWINN-HARDY, K, SORENSEN, B, CONSIDINE, E, TUCKER, S, LYNCH, D. R, MATHEWS, K. D, SWOBODA, K. J, HARRIS, J

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Steroid therapy and cardiac function in Duchenne muscular dystrophy von Markham, L W, Spicer, R L, Khoury, P R, Wong, B L, Mathews, K D, Cripe, L H

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Aberrant regulation of epigenetic modifiers contributes to the pathogenesis in patients with selenoprotein N‐related myopathies von Bachmann, Christoph, Noreen, Faiza, Voermans, Nicol C., Schär, Primo L., Vissing, John, Fock, Johanna M., Bulk, Saskia, Kusters, Benno, Moore, Steven A., Beggs, Alan H., Mathews, Katherine D., Meyer, Megan, Genetti, Casie A., Meola, Giovanni, Cardani, Rosanna, Mathews, Emma, Jungbluth, Heinz, Muntoni, Francesco, Zorzato, Francesco, Treves, Susan

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Post-translational disruption of dystroglycan-ligand interactions in congenital muscular dystrophies von Campbell, Kevin P, Michele, Daniel E, Barresi, Rita, Kanagawa, Motoi, Saito, Fumiaki, Cohn, Ronald D, Satz, Jakob S, Dollar, James, Nishino, Ichizo, Kelley, Richard I, Somer, Hannu, Straub, Volker, Mathews, Katherine D, Moore, Steven A

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Meta-analyses of ataluren randomized controlled trials in nonsense mutation Duchenne muscular dystrophy von Campbell, Craig, Barohn, Richard J, Bertini, Enrico, Chabrol, Brigitte, Comi, Giacomo Pietro, Darras, Basil T, Finkel, Richard S, Flanigan, Kevin M, Goemans, Nathalie, Iannaccone, Susan T, Jones, Kristi J, Kirschner, Janbernd, Mah, Jean K, Mathews, Katherine D, McDonald, Craig M, Mercuri, Eugenio, Nevo, Yoram, Péréon, Yann, Renfroe, J Ben, Ryan, Monique M, Sampson, Jacinda B, Schara, Ulrike, Sejersen, Thomas, Selby, Kathryn, Tulinius, Már, Vílchez, Juan J, Voit, Thomas, Wei, Lee-Jen, Wong, Brenda L, Elfring, Gary, Souza, Marcio, McIntosh, Joseph, Trifillis, Panayiota, Peltz, Stuart W, Muntoni, Francesco

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Myoglobinuria and muscle pain are common in patients with limb-girdle muscular dystrophy 2I von Mathews, K D, Stephan, C M, Laubenthal, K, Winder, T L, Michele, D E, Moore, S A, Campbell, K P

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MYOGLOBINURIA AND MUSCLE PAIN ARE COMMON IN PATIENTS WITH LIMB-GIRDLE MUSCULAR DYSTROPHY 21 von MATHEWS, K. D, STEPHAN, C. M, LAUBENTHAL, K, WINDER, T. L, MICHELE, D. E, MOORE, S. A, CAMPBELL, K. P

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FSH dystrophy 4q35 deletion in patients presenting with facial-sparing scapular myopathy von FELICE, K. J, NORTH, W. A, MOORE, S. A, MATHEWS, K. D

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Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and pharmacological and psychosocial management von Bushby, Katharine, MD, Finkel, Richard, MD, Birnkrant, David J, MD, Case, Laura E, DPT, Clemens, Paula R, MD, Cripe, Linda, MD, Kaul, Ajay, MD, Kinnett, Kathi, MSN, McDonald, Craig, MD, Pandya, Shree, PT, Poysky, James, PhD, Shapiro, Frederic, MD, Tomezsko, Jean, PhD, Constantin, Carolyn, PhD

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Spinal muscular atrophy care in the COVID‐19 pandemic era von Veerapandiyan, Aravindhan, Connolly, Anne M., Finkel, Richard S., Arya, Kapil, Mathews, Katherine D., Smith, Edward C., Castro, Diana, Butterfield, Russell J., Parsons, Julie A., Servais, Laurent, Kuntz, Nancy, Rao, Vamshi K., Brandsema, John F., Mercuri, Eugenio, Ciafaloni, Emma

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Consensus-based care recommendations for adults with myotonic dystrophy type 1 von Ashizawa, Tetsuo, Gagnon, Cynthia, Groh, William J, Gutmann, Laurie, Johnson, Nicholas E, Meola, Giovanni, Moxley, 3rd, Richard, Pandya, Shree, Rogers, Mark T, Simpson, Ericka, Angeard, Nathalie, Bassez, Guillaume, Berggren, Kiera N, Bhakta, Deepak, Bozzali, Marco, Broderick, Ann, Byrne, Janice L B, Campbell, Craig, Cup, Edith, Day, John W, De Mattia, Elisa, Duboc, Denis, Duong, Tina, Eichinger, Katy, Ekstrom, Anne-Berit, van Engelen, Baziel, Esparis, Belen, Eymard, Bruno, Ferschl, Marla, Gadalla, Shahinaz M, Gallais, Benjamin, Goodglick, Todd, Heatwole, Chad, Hilbert, James, Holland, Venessa, Kierkegaard, Marie, Koopman, Wilma J, Lane, Kari, Maas, Daphne, Mankodi, Ami, Mathews, Katherine D, Monckton, Darren G, Moser, David, Nazarian, Saman, Nguyen, Linda, Nopoulos, Peg, Petty, Richard, Phetteplace, Janel, Puymirat, Jack, Raman, Subha, Richer, Louis, Roma, Elisabetta, Sampson, Jacinda, Sansone, Valeria, Schoser, Benedikt, Sterling, Laurie, Statland, Jeffrey, Subramony, S H, Tian, Cuixia, Trujillo, Careniña, Tomaselli, Gordon, Turner, Chris, Venance, Shannon, Verma, Aparajitha, White, Molly, Winblad, Stefan

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Prevalence of Duchenne and Becker muscular dystrophies in the United States von Romitti, Paul A, Zhu, Yong, Puzhankara, Soman, James, Katherine A, Nabukera, Sarah K, Zamba, Gideon K D, Ciafaloni, Emma, Cunniff, Christopher, Druschel, Charlotte M, Mathews, Katherine D, Matthews, Dennis J, Meaney, F John, Andrews, Jennifer G, Conway, Kristin M Caspers, Fox, Deborah J, Street, Natalie, Adams, Melissa M, Bolen, Julie

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Diagnostic approach to the congenital muscular dystrophies von Bönnemann, Carsten G, Wang, Ching H, Quijano-Roy, Susana, Deconinck, Nicolas, Bertini, Enrico, Ferreiro, Ana, Muntoni, Francesco, Sewry, Caroline, Béroud, Christophe, Mathews, Katherine D, Moore, Steven A, Bellini, Jonathan, Rutkowski, Anne, North, Kathryn N

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Genetic and physical mapping on chromosome 4 narrows the localization of the gene for facioscapulohumeral muscular dystrophy (FSHD) von MILLS, K. A, BUETOW, K. H, XU, Y, RITTY, T. M, MATHEWS, K. D, BODRUG, S. E, WIJMENGA, C, BALAZS, I, MURRAY, J. C

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Reflex sympathetic dystrophy in children von DIETZ, F. R, MATHEWS, K. D, MONTGOMERY, W. J

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Linkage localization of facioscapulohumeral muscular dystrophy (FSHD) in 4q35 von MATHEWS, K. D, MILLS, K. A, BOSCH, E. P, IONASESCU, V. V, WILES, K. R, BUETOW, K. H, MURRAY, J. C

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Genetic and Physical Mapping of a Voltage-Dependent Chloride Channel Gene to Human 4q32 and to Mouse 8 von Mills, Kathleen A., Mathews, Katherine D., Scherpbier-Heddema, Titia, Buetow, Kenneth H., Baldini, Antonio, Ballabio, Andrea, Borsani, Giuseppe

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SMA-MAP: a plasma protein panel for spinal muscular atrophy von Kobayashi, Dione T, Shi, Jing, Stephen, Laurie, Ballard, Karri L, Dewey, Ruth, Mapes, James, Chung, Brett, McCarthy, Kathleen, Swoboda, Kathryn J, Crawford, Thomas O, Li, Rebecca, Plasterer, Thomas, Joyce, Cynthia, Chung, Wendy K, Kaufmann, Petra, Darras, Basil T, Finkel, Richard S, Sproule, Douglas M, Martens, William B, McDermott, Michael P, De Vivo, Darryl C, Walker, Michael G, Chen, Karen S

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The Ant1 gene maps near Klk3 on proximal mouse chromosome 8 von Mills, K A, Ellison, J W, Mathews, K D

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Drug-Drug Interaction Between Clopidogrel and the Proton Pump Inhibitors von Norgard, Nicholas B, Mathews, Kathryn D, Wall, Geoffrey C

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